Clearance Summary
AMERICAN DENTAL IMPLANT received FDA 510(k) clearance under submission number K042462, sponsored by American Dental Implant Corporation. The device was reviewed via the Traditional premarket notification pathway and assigned to the Dental review panel. The statutory decision date of record is 2004-09-21.
- Submission: K042462
- Applicant / Sponsor: American Dental Implant Corporation
- Clearance pathway: Traditional
- Review panel: Dental
- Device class: Class II
- Regulation citation: 21 CFR 872.3640
- Decision date: 2004-09-21
Classification & Regulation
This clearance is catalogued under FDA product code DZE and 21 CFR 872.3640, within the Dental review panel as a Class II device.